Variant report

Variant	esv1799856
Chromosome Location	chr1:155305059-155534616
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2072)
CpG islands
(count:1588)
Chromatin interactive
region (count:178)
LncRNA
region (count:16)
Mature miRNA
region (count: 1)
miRNA target
sites (count:8)

(count:2072 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:155506048-155506168	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:155506925-155506970	K562	blood:	n/a	n/a
3	ARID3A	chr1:155474133-155474294	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:155505882-155506410	K562	blood:	n/a	n/a
5	ARID3A	chr1:155474099-155474299	K562	blood:	n/a	n/a
6	ARID3A	chr1:155359836-155359982	K562	blood:	n/a	n/a
7	ARID3A	chr1:155427977-155428203	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:155484415-155484565	K562	blood:	n/a	n/a
9	ARID3A	chr1:155533549-155533937	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:155532749-155533151	K562	blood:	n/a	n/a
11	ATF1	chr1:155313764-155313791	K562	blood:	n/a	n/a
12	ATF1	chr1:155484415-155484621	K562	blood:	n/a	n/a
13	ATF1	chr1:155506118-155506352	K562	blood:	n/a	n/a
14	ATF2	chr1:155499663-155500136	GM12878	blood:	n/a	n/a
15	ATF2	chr1:155505799-155506524	GM12878	blood:	n/a	n/a
16	ATF2	chr1:155515946-155516309	GM12878	blood:	n/a	n/a
17	ATF2	chr1:155436003-155436471	GM12878	blood:	n/a	n/a
18	ATF2	chr1:155499591-155500176	GM12878	blood:	n/a	n/a
19	ATF2	chr1:155532596-155533085	GM12878	blood:	n/a	n/a
20	ATF2	chr1:155532606-155533273	GM12878	blood:	n/a	n/a
21	ATF2	chr1:155517338-155517651	GM12878	blood:	n/a	n/a
22	ATF2	chr1:155469998-155470523	GM12878	blood:	n/a	n/a
23	ATF2	chr1:155435971-155436530	GM12878	blood:	n/a	n/a
24	ATF3	chr1:155532408-155532643	K562	blood:	n/a	n/a
25	ATF3	chr1:155532730-155533195	A549	lung:	n/a	n/a
26	BACH1	chr1:155532778-155532882	K562	blood:	n/a	n/a
27	BACH1	chr1:155508706-155508758	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr1:155532759-155533072	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr1:155435621-155435850	GM12878	blood:	n/a	chr1:155435817-155435827
30	BATF	chr1:155509775-155510116	GM12878	blood:	n/a	n/a
31	BATF	chr1:155505851-155506378	GM12878	blood:	n/a	n/a
32	BATF	chr1:155509822-155510076	GM12878	blood:	n/a	n/a
33	BATF	chr1:155516056-155516237	GM12878	blood:	n/a	n/a
34	BATF	chr1:155433644-155433937	GM12878	blood:	n/a	chr1:155433820-155433831 chr1:155433821-155433831
35	BATF	chr1:155533838-155534037	GM12878	blood:	n/a	chr1:155533977-155533986
36	BATF	chr1:155531493-155531877	GM12878	blood:	n/a	n/a
37	BATF	chr1:155532878-155533223	GM12878	blood:	n/a	n/a
38	BATF	chr1:155510129-155510431	GM12878	blood:	n/a	n/a
39	BATF	chr1:155533808-155534078	GM12878	blood:	n/a	chr1:155533977-155533986
40	BATF	chr1:155510154-155510430	GM12878	blood:	n/a	n/a
41	BATF	chr1:155433658-155433999	GM12878	blood:	n/a	chr1:155433820-155433831 chr1:155433821-155433831
42	BATF	chr1:155515911-155516329	GM12878	blood:	n/a	n/a
43	BCL11A	chr1:155531434-155531867	GM12878	blood:	n/a	n/a
44	BCL11A	chr1:155532354-155532627	GM12878	blood:	n/a	n/a
45	BCL11A	chr1:155532829-155533461	GM12878	blood:	n/a	n/a
46	BCL11A	chr1:155531636-155531849	GM12878	blood:	n/a	n/a
47	BCL11A	chr1:155515924-155516242	GM12878	blood:	n/a	n/a
48	BCL3	chr1:155532730-155533206	A549	lung:	n/a	n/a
49	BCL3	chr1:155532620-155533261	A549	lung:	n/a	n/a
50	BCL3	chr1:155460228-155460557	GM12878	blood:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155316648-155316698	K562	blood:	n/a
2	chr1:155532814-155532864	CMK	blood:	n/a
3	chr1:155316648-155316698	K562	blood:	n/a
4	chr1:155532814-155532864	CMK	blood:	n/a
5	chr1:155510764-155510814	AoSMC	blood vessel:	n/a
6	chr1:155530669-155530719	HMEC	breast:	n/a
7	chr1:155532716-155532766	NT2-D1	testis:	n/a
8	chr1:155317652-155317702	Caco-2	colon:	n/a
9	chr1:155532722-155532772	AG09309	skin:	n/a
10	chr1:155529057-155529107	AG04449	skin:	fetal
11	chr1:155317652-155317702	HNPCEpiC	eye:	n/a
12	chr1:155530669-155530719	U87	brain:	n/a
13	chr1:155533016-155533066	BJ	skin:	n/a
14	chr1:155530669-155530719	ECC-1	luminal epithelium:	n/a
15	chr1:155533405-155533455	BJ	skin:	n/a
16	chr1:155317515-155317565	A549	lung:	n/a
17	chr1:155532420-155532470	HUVEC	blood vessel:	n/a
18	chr1:155532420-155532470	NH-A	brain:	n/a
19	chr1:155470302-155470352	PANC-1	pancreas:	n/a
20	chr1:155532099-155532149	HepG2	liver:	n/a
21	chr1:155448900-155448950	HIPEpiC	eye:	n/a
22	chr1:155532099-155532149	NH-A	brain:	n/a
23	chr1:155470302-155470352	HEK293	kidney:	embryo
24	chr1:155317625-155317675	Caco-2	colon:	n/a
25	chr1:155348145-155348195	IMR90	lung:	fetal
26	chr1:155317515-155317565	SAEC	small airway:	n/a
27	chr1:155532722-155532772	HRE	kidney:	n/a
28	chr1:155348145-155348195	H1-hESC	embryonic stem cell:	embryo
29	chr1:155448900-155448950	H1-hESC	embryonic stem cell:	embryo
30	chr1:155533405-155533455	GM06990	blood:	n/a
31	chr1:155448900-155448950	AG09309	skin:	n/a
32	chr1:155317652-155317702	ProgFib	skin:	n/a
33	chr1:155317515-155317565	PFSK-1	brain:	n/a
34	chr1:155533016-155533066	NT2-D1	testis:	n/a
35	chr1:155533405-155533455	ProgFib	skin:	n/a
36	chr1:155530669-155530719	K562	blood:	n/a
37	chr1:155317515-155317565	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:155305329-155305379	Caco-2	colon:	n/a
39	chr1:155305329-155305379	HRE	kidney:	n/a
40	chr1:155534509-155534559	HCF	heart:	n/a
41	chr1:155316648-155316698	H1-hESC	embryonic stem cell:	embryo
42	chr1:155484600-155484650	GM19239	blood:	n/a
43	chr1:155470302-155470352	HCF	heart:	n/a
44	chr1:155317402-155317452	HNPCEpiC	eye:	n/a
45	chr1:155534509-155534559	AG09309	skin:	n/a
46	chr1:155532420-155532470	PFSK-1	brain:	n/a
47	chr1:155317402-155317452	HRPEpiC	eye:	n/a
48	chr1:155348145-155348195	RPTEC	kidney:	n/a
49	chr1:155533819-155533869	HMEC	breast:	n/a
50	chr1:155532420-155532470	HMEC	breast:	n/a

(count:178 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:155473489..155475636-chr1:155495216..155497705,2	K562	blood:
2	chr1:155532787..155533321-chr1:155658619..155659301,2	Hela-S3	cervix:
3	chr1:155502169..155504440-chr1:155504548..155506346,2	K562	blood:
4	chr1:155290754..155293213-chr1:155329435..155331976,2	K562	blood:
5	chr1:155163156..155164893-chr1:155532696..155534228,2	K562	blood:
6	chr1:155531220..155534536-chr1:155656727..155659727,4	MCF-7	breast:
7	chr1:155518733..155520957-chr1:155531970..155533886,3	MCF-7	breast:
8	chr1:155495388..155497007-chr1:155499838..155502620,2	K562	blood:
9	chr1:155473858..155476740-chr1:155479464..155482113,2	K562	blood:
10	chr1:155315148..155318392-chr1:155319854..155323114,3	K562	blood:
11	chr1:155533054..155535636-chr1:155540451..155542741,3	MCF-7	breast:
12	chr1:155322221..155325008-chr1:155325943..155327499,2	K562	blood:
13	chr1:155407176..155408712-chr1:155532541..155534378,2	K562	blood:
14	chr1:155403382..155405033-chr1:155410583..155412465,2	MCF-7	breast:
15	chr1:155406981..155408656-chr1:155410586..155413532,3	K562	blood:
16	chr1:155532724..155534552-chr1:155658209..155659716,2	K562	blood:
17	chr1:155293363..155295727-chr1:155310935..155312510,2	MCF-7	breast:
18	chr1:155300511..155303524-chr1:155305047..155307962,3	K562	blood:
19	chr1:155515123..155516751-chr1:155518229..155520360,2	K562	blood:
20	chr1:155447924..155449815-chr1:155468121..155471028,2	K562	blood:
21	chr1:155515123..155516751-chr1:155518229..155520360,2	K562	blood:
22	chr1:155486468..155488320-chr1:155531451..155534775,4	K562	blood:
23	chr1:155302374..155305102-chr1:155305552..155308800,4	MCF-7	breast:
24	chr1:155517271..155518902-chr1:155523371..155525530,2	K562	blood:
25	chr1:155430681..155432284-chr1:155445410..155448116,2	MCF-7	breast:
26	chr1:155470186..155472213-chr1:155476208..155478558,2	K562	blood:
27	chr1:155428479..155431081-chr1:155533087..155535825,2	K562	blood:
28	chr1:155292800..155294999-chr1:155531525..155533061,2	K562	blood:
29	chr1:155431476..155435286-chr1:155435557..155439516,4	K562	blood:
30	chr1:155516947..155518463-chr1:155526285..155527912,2	K562	blood:
31	chr1:155428479..155431081-chr1:155533087..155535825,2	K562	blood:
32	chr1:155477742..155481742-chr1:155532390..155535967,3	MCF-7	breast:
33	chr1:155148862..155150825-chr1:155499842..155501461,2	MCF-7	breast:
34	chr1:155495388..155497007-chr1:155499838..155502620,2	K562	blood:
35	chr1:155430681..155432284-chr1:155445410..155448116,2	MCF-7	breast:
36	chr1:155532088..155534231-chr8:145750623..145753092,2	MCF-7	breast:
37	chr1:155533061..155533901-chr6:32939793..32940739,2	NB4	blood:
38	chr1:155532081..155532969-chr1:155658202..155658825,5	HCT-116	colon:
39	chr1:155491837..155494336-chr1:155496208..155498633,2	K562	blood:
40	chr1:155424741..155427653-chr1:155526371..155528510,2	K562	blood:
41	chr1:155305056..155307139-chr1:155312241..155314474,2	MCF-7	breast:
42	chr1:155311963..155313733-chr1:155337378..155340313,2	MCF-7	breast:
43	chr1:155497441..155500287-chr1:155501930..155504131,2	K562	blood:
44	chr1:155503214..155505197-chr1:155523431..155525901,2	K562	blood:
45	chr1:155444793..155446300-chr1:155452927..155455917,2	MCF-7	breast:
46	chr1:155473340..155475715-chr1:155533931..155535804,2	K562	blood:
47	chr1:155339400..155342003-chr1:155343573..155345841,2	K562	blood:
48	chr1:155444057..155446156-chr1:155448609..155450832,2	K562	blood:
49	chr1:155532611..155533379-chr11:17229191..17230143,2	Hela-S3	cervix:
50	chr1:155457376..155459656-chr1:155466339..155468887,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PKLR-7	chr1:155360786-155361172	expReg_chr1_16541_-
2	lnc-PKLR-2	chr1:155366715-155366769	ENSG00000227773.1
3	lnc-MSTO1-1	chr1:155531821-155533775	ENSG00000235919.3
4	lnc-RUSC1-2	chr1:155423375-155423819	NONHSAT006739
5	lnc-YY1AP1-6	chr1:155473462-155473550	NONHSAT006740
6	lnc-MSTO1-1	chr1:155531772-155533735	NONHSAT006742
7	lnc-YY1AP1-6	chr1:155468645-155468954	NONHSAT006740
8	lnc-MSTO1-1	chr1:155533041-155533735	ENSG00000235919
9	lnc-PKLR-2	chr1:155365801-155366193	ENSG00000227773.1
10	lnc-PKLR-6	chr1:155359921-155360669	expReg_chr1_16540_-
11	lnc-MSTO1-1	chr1:155531833-155532077	ENSG00000235919
12	lnc-PKLR-5	chr1:155358957-155359511	expReg_chr1_16538_-
13	lnc-PKLR-4	chr1:155358178-155358389	expReg_chr1_16535_-
14	lnc-MSTO1-1	chr1:155531864-155532077	ENSG00000235919
15	lnc-RUSC1-2	chr1:155421802-155421827	NONHSAT006739
16	lnc-MSTO1-1	chr1:155532772-155533437	ENSG00000235919

miRNA name	Chromosome Location	mirBase accession
hsa-miR-555	chr1:155316156-155316176	MIMAT0003219

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ASH1L	hsa-miR-17-5p	chr1:155305669-155305663
2	ASH1L	hsa-miR-103a-3p	chr1:155305221-155305242
3	ASH1L	hsa-miR-103a-3p	chr1:155305227-155305221
4	ASH1L	hsa-miR-16-5p	chr1:155306654-155306676
5	ASH1L	hsa-miR-16-5p	chr1:155305226-155305219
6	ASH1L	hsa-miR-16-5p	chr1:155305220-155305241
7	ASH1L	hsa-miR-185-5p	chr1:155307231-155307255
8	ASH1L	hsa-miR-185-5p	chr1:155306918-155306938

Variant related genes	Relation type
POU5F1P4	TF binding region
ENSG00000238805	TF binding region
ASH1L-IT1	TF binding region
MIR555	TF binding region
RNU6-106P	TF binding region
RNU6-1297P	TF binding region
ASH1L-AS1	TF binding region
ASH1L	TF binding region
POU5F1P4	CpG island
ENSG00000238805	CpG island
ASH1L-IT1	CpG island
MIR555	CpG island
RNU6-106P	CpG island
RNU6-1297P	CpG island
ASH1L-AS1	CpG island
ASH1L	CpG island
ENSG00000092841	chromatin interactions
ENSG00000207720	chromatin interactions
ENSG00000166454	chromatin interactions
ENSG00000124693	chromatin interactions
ENSG00000172270	chromatin interactions
ENSG00000166716	chromatin interactions
ENSG00000254402	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000143630	chromatin interactions
ENSG00000011405	chromatin interactions
ENSG00000271748	chromatin interactions
ENSG00000263756	chromatin interactions
ENSG00000163462	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000238805	chromatin interactions
ENSG00000116521	chromatin interactions
ENSG00000132676	chromatin interactions
ENSG00000267751	chromatin interactions
ENSG00000235919	chromatin interactions
ENSG00000163374	chromatin interactions
ENSG00000271267	chromatin interactions
ENSG00000123975	chromatin interactions
ENSG00000267064	chromatin interactions
ENSG00000160767	chromatin interactions
ENSG00000257809	chromatin interactions
ENSG00000163348	chromatin interactions
ENSG00000197980	chromatin interactions
ENSG00000070081	chromatin interactions
ENSG00000260213	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000116539	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000108946	chromatin interactions
ENSG00000227773	chromatin interactions
ENSG00000163463	chromatin interactions
ENSG00000126756	chromatin interactions

Extended variants
information (count: 7972 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:7972 , 50 per page) page: 1 2 3 4 5 6 7 ... 160

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6695298	chr1:155305059-155305060	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs559164769	chr1:155305136-155305137	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534050517	chr1:155305240-155305241	Weak transcription Strong transcription	Chromatin interactive region miRNA target site	3 gene(s)	Overlapped CNVs	n/a
4	rs546343375	chr1:155305272-155305273	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs376484962	chr1:155305275-155305276	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs11552268	chr1:155305290-155305291	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs528257452	chr1:155305309-155305310	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs182414333	chr1:155305361-155305362	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs186687102	chr1:155305398-155305399	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs551684330	chr1:155305408-155305409	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs111566986	chr1:155305456-155305457	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs577959889	chr1:155305477-155305478	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs556974313	chr1:155305530-155305531	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs575525964	chr1:155305574-155305575	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs535858205	chr1:155305594-155305595	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs554618295	chr1:155305655-155305656	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs1047304	chr1:155305677-155305678	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs376985314	chr1:155305721-155305722	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs540331849	chr1:155305736-155305737	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs565437200	chr1:155305746-155305747	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs571425788	chr1:155305791-155305792	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs192524983	chr1:155305802-155305803	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs540520123	chr1:155305849-155305850	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs537465700	chr1:155305878-155305879	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs71845643	chr1:155305879-155305880	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs544836032	chr1:155305896-155305897	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs563018264	chr1:155305903-155305904	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs114579766	chr1:155305928-155305929	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs541830197	chr1:155305959-155305960	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs77675900	chr1:155306009-155306010	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs148609149	chr1:155306021-155306022	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs552245373	chr1:155306022-155306023	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs116580423	chr1:155306064-155306065	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs185736856	chr1:155306127-155306128	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs114319471	chr1:155306140-155306141	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs116477839	chr1:155306142-155306143	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs532188574	chr1:155306144-155306145	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs141035761	chr1:155306149-155306150	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs148726843	chr1:155306151-155306152	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs373321279	chr1:155306152-155306153	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs113407669	chr1:155306162-155306163	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs562925292	chr1:155306189-155306190	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs114130331	chr1:155306195-155306196	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs541142167	chr1:155306196-155306197	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs41264227	chr1:155306197-155306198	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs576341576	chr1:155306203-155306204	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs528864992	chr1:155306236-155306237	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs536573244	chr1:155306359-155306360	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs41264229	chr1:155306440-155306441	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs141175258	chr1:155306460-155306461	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:6961 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155295000-155307000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr1:155295000-155307000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr1:155295200-155306000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr1:155295400-155307400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr1:155295400-155308600	Weak transcription	Psoas Muscle	Psoas
6	chr1:155295800-155306600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr1:155295800-155307200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr1:155296000-155307200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr1:155296000-155309000	Weak transcription	Stomach Mucosa	stomach
10	chr1:155296000-155334400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:155296200-155312800	Weak transcription	Fetal Heart	heart
12	chr1:155296200-155349400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:155296600-155348200	Strong transcription	Fetal Stomach	stomach
14	chr1:155296800-155305200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr1:155296800-155330000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:155297000-155330800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:155297200-155322600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr1:155297800-155357400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:155298200-155320800	Strong transcription	Fetal Thymus	thymus
20	chr1:155299600-155330200	Strong transcription	Rectal Mucosa Donor 29	rectum
21	chr1:155299600-155341200	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr1:155299600-155353600	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr1:155300600-155306600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr1:155300800-155306800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr1:155300800-155311600	Weak transcription	Small Intestine	intestine
26	chr1:155301000-155306800	Weak transcription	Fetal Brain Male	brain
27	chr1:155301000-155307000	Weak transcription	NHEK	skin
28	chr1:155301000-155307000	Weak transcription	NHLF	lung
29	chr1:155301200-155306400	Weak transcription	K562	blood
30	chr1:155301200-155306800	Weak transcription	Brain Hippocampus Middle	brain
31	chr1:155301200-155306800	Weak transcription	A549	lung
32	chr1:155301200-155306800	Weak transcription	HSMMtube	muscle
33	chr1:155301200-155307000	Weak transcription	Colonic Mucosa	Colon
34	chr1:155301200-155307400	Weak transcription	HMEC	breast
35	chr1:155301200-155332200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr1:155301400-155306400	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr1:155301400-155306600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr1:155301400-155306600	Weak transcription	Aorta	Aorta
39	chr1:155301400-155306800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr1:155301400-155306800	Weak transcription	Gastric	stomach
41	chr1:155301400-155306800	Weak transcription	Ovary	ovary
42	chr1:155301400-155306800	Weak transcription	Rectal Smooth Muscle	rectum
43	chr1:155301400-155307000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr1:155301400-155307000	Weak transcription	Pancreas	Pancrea
45	chr1:155301400-155311800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr1:155301600-155306400	Weak transcription	Colon Smooth Muscle	Colon
47	chr1:155301600-155306800	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr1:155301600-155306800	Weak transcription	Lung	lung
49	chr1:155301600-155311600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr1:155301800-155306600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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